Shoulder iD DWJ608Recalls & reported problems
Tornier, Inc. · Primary Reversed Glenoid · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840338604231), received between Jul 25, 2024 and Mar 19, 2026 — classified as 2 injuries.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Fever1
- Implant Pain1
- Joint Impingement1
- Muscle/Tendon Damage1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2026Adverse Event Without Identified Device or Use Problem
SUBJECT: (B)(6). SHOULDER ID STUDY. NARRATIVE: PATIENT CALLED THE CLINIC TO REPORT PAIN AND A POTENTIAL SHOULDER DISLOCATION. HE STATES HE RAISED HIS ARM OVERHEAD TOO QUICKLY. AFTER SEEING THE PATIENT, THE SURGEON REPORTED BEING CONCERNED FOR EITHER A DELTOID STRAIN OR ACROMIAL STRESS FRACTURE. THE SURGEON ADVISED THE PATIENT TO REST AND RETURN TO THE CLINIC IN TWO WEEKS WITH NEW IMAGES, AND SHE WILL FURTHER ASSESS HIM AT THAT TIME.
Patient problems: Muscle/Tendon Damage; Pain
MAUDE report 24637893 ↗InjuryJul 25, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SUBJECT: (B)(6). SHOULDER ID STUDY. AS REPORTED: PATIENT REPORTED A "CATCHING" FEELING IN SHOULDER WITH INCREASED PAIN SINCE (B)(6) 2024. PT ALSO HAD A FEVER ON (B)(6) 2024; ANTIBIOTICS WERE PRESCRIBED FOR THIS. AS OF (B)(6) 2024, THE PATIENT REPORTED THAT HER SHOULDER PAIN IS IMPROVING.
Patient problems: Fever; Implant Pain; Joint Impingement
MAUDE report 19833648 ↗
Other shoulder prosthesis, reverse configuration devices
- DJO SURGICAL 508-36-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration508 reports
- DJO SURGICAL 508-32-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration433 reports
- DJO SURGICAL 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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